NDC 82160-276 Photoblock Plus

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82160-276
Proprietary Name:
Photoblock Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
82160
Start Marketing Date: [9]
03-15-2011
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 82160-276?

The NDC code 82160-276 is assigned by the FDA to the product Photoblock Plus which is product labeled by Pella Pharmaceuticals Co. Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82160-276-01 1 tube in 1 carton / 75 g in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Photoblock Plus?

Photoblock ® Plus Cream is used to provide maximum sun protection while maintaining a youthful and radiant skin. Photoblock ® Plus Cream protects the skin against premature aging caused by exposure to UVA due to its components Ronacare AP and Parsol 1789 (A vobenzone ), the only substances approved by the American FDA "Food and Drug Administration", which provide complete protection against UVA. It also contains Titanium Dioxide which provides protection against UVB rays that cause redness and burns.

Which are Photoblock Plus UNII Codes?

The UNII codes for the active ingredients in this product are:

  • AVOBENZONE (UNII: G63QQF2NOX)
  • AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
  • BIS-ETHYLHEXYL HYDROXYDIMETHOXY BENZYLMALONATE (UNII: 7D4Q5YJ8NV)
  • BIS-ETHYLHEXYL HYDROXYDIMETHOXY BENZYLMALONATE (UNII: 7D4Q5YJ8NV) (Active Moiety)

Which are Photoblock Plus Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".